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Dr. Diana, both a doctor (therapeutic optometrist), and a recovered POTS and ME/CFS patient, offers help and hope for POTS, Dysautonomia, Ehlers-Danlos syndrome, Chronic Fatigue, Chronic Lyme, vascular abnormalities, Fibromyalgia, and Multiple Sclerosis. Dr. Diana is now working full time at POTS Care.
NEW STUDY! Parasym Plus™ for Multiple Sclerosis › Forums › PrettyIll.com Discussion › EDS/MS/Chiari › Who is the right specialty to see for EDS diagnosis?
My son is interested in being tested for EDS. He already went through genetic testing for Marfan Syndrome and didn’t have “enough” symptoms for a positive diagnosis; however, he seems to fall into the possibility of EDS. I’m just curious, who would be the right speciality to be sent to for appropriate testing? We had Kaiser before, and now we don’t. We have Private Ins.
Thank you! I didn’t think about that! Duh, me!
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“Dr. Diana will always hold a very special place in my heart for her selfless devotion to helping everyone, not just the Ehlers-Danlos community. I hate to think what my life would be without her insight and guidance.”
-- Chris Gross